Seedless monordica grosvenori and cultivating method thereof
A cultivation method and technology of Luo Han Guo, applied in horticultural methods, botanical equipment and methods, plant cells, etc., to achieve the effects of high utilization rate of the whole fruit, enhanced matability, and high content
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Embodiment 1
[0020] Set the indoor cultivation temperature at 15-24°C, and perform indoor operations under sterile conditions;
[0021] 1) taking explants of diploid Luo Han Guo female and male plant explants activated by flowering factors, and breeding tissue culture seedlings according to conventional methods;
[0022] 2) Select tissue-cultured subcultured seedlings with strong growth potential, cause wounds in different parts, wrap them tightly with absorbent cotton, drip colchicine solution with a mass concentration of 0.03% on the absorbent cotton for 10 days, and wash with sterile water;
[0023] 3) Cut out different parts of the female and male plants after the induction treatment, and transfer them to the differentiation medium for dark culture for 10 days, then light culture for 20 days, light for 8-12 hours per day, and the light intensity is 1000-2000LX;
[0024] 4) cutting out the stem tips and stem segments of the new shoots grown after the above-mentioned cultivation and tran...
Embodiment 2
[0030] Set the indoor cultivation temperature at 24-32°C, and perform indoor operations under sterile conditions;
[0031] 1) taking explants of diploid Luo Han Guo female and male plant explants activated by flowering factors, and breeding tissue culture seedlings according to conventional methods;
[0032] 2) select the subcultured seedlings for tissue culture, soak their terminal buds with a colchicine solution with a mass concentration of 0.8% for 3 days, and wash them with sterile water;
[0033] 3) Cut out the different parts of the induced female and male plants, and transfer them to the differentiation medium for dark culture for 5 days, then light culture for 20 days, with 12-16 hours of light per day, and the light intensity is 2000-3600LX ;
[0034] 4) Cut out the stem tips and stem segments of the sprouts grown after the above culture and transfer them to the callus culture medium to induce callus production and proliferation, cut the callus into small pieces, and...
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